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咪喹莫特通过诱导免疫原性细胞死亡发挥抗肿瘤作用,并被糖酵解抑制剂 2-脱氧葡萄糖增强。

Imiquimod Exerts Antitumor Effects by Inducing Immunogenic Cell Death and Is Enhanced by the Glycolytic Inhibitor 2-Deoxyglucose.

机构信息

Center for Cell Therapy and Translation Research, China Medical University Hospital, Taichung, Taiwan.

Department of Dermatology, Taichung Veterans General Hospital, Taichung, Taiwan.

出版信息

J Invest Dermatol. 2020 Sep;140(9):1771-1783.e6. doi: 10.1016/j.jid.2019.12.039. Epub 2020 Feb 6.

DOI:10.1016/j.jid.2019.12.039
PMID:32035924
Abstract

The induction of immunogenic cell death (ICD) in cancer cells triggers specific immune responses against the same cancer cells. Imiquimod (IMQ) is a synthetic ligand of toll-like receptor 7 that exerts antitumor activity by stimulating cell-mediated immunity or by directly inducing apoptosis. Whether IMQ causes tumors to undergo ICD and elicits a specific antitumor immune response is unknown. We demonstrated that IMQ-induced ICD-associated features, including the surface exposure of calreticulin and the secretion of adenosine triphosphate and HMGB1, were mediated by ROS and endoplasmic reticulum stress. In a B16F10 melanoma mouse model, vaccinating mice with IMQ-induced ICD cell lysate or directly injecting IMQ in situ reduced tumor growth that was mediated by inducing tumor-specific T-cell proliferation, promoting tumor-specific cytotoxic killing by CD8 T cells, and increasing the infiltration of various immune cells into tumor lesions. The ICD-associated features were crucial in the induction of specific antitumor immunity in vivo. The glycolytic inhibitor 2-deoxyglucose enhanced IMQ-induced ICD-associated features and strengthened the antitumor immunity mediated by IMQ-induced ICD cell lysate in p53-mutant cancer cells, which were IMQ-resistant in vitro. We conclude that IMQ is an authentic ICD inducer and provide a concept connecting IMQ-induced cancer cell death and antitumor immune responses.

摘要

诱导癌细胞发生免疫原性细胞死亡 (ICD) 会引发针对同一癌细胞的特异性免疫反应。咪喹莫特 (IMQ) 是 Toll 样受体 7 的合成配体,通过刺激细胞介导的免疫或直接诱导细胞凋亡发挥抗肿瘤活性。IMQ 是否导致肿瘤发生 ICD 并引发特异性抗肿瘤免疫反应尚不清楚。我们证明,IMQ 诱导的 ICD 相关特征,包括钙网蛋白的表面暴露以及三磷酸腺苷和高迁移率族蛋白 B1 的分泌,是由 ROS 和内质网应激介导的。在 B16F10 黑色素瘤小鼠模型中,用 IMQ 诱导的 ICD 细胞裂解物对小鼠进行疫苗接种或直接原位注射 IMQ 可减少肿瘤生长,其机制是诱导肿瘤特异性 T 细胞增殖、促进 CD8 T 细胞对肿瘤的特异性细胞毒性杀伤以及增加各种免疫细胞浸润肿瘤病变。ICD 相关特征在体内诱导特异性抗肿瘤免疫中至关重要。糖酵解抑制剂 2-脱氧葡萄糖增强了 IMQ 诱导的 ICD 相关特征,并增强了 p53 突变型癌细胞中由 IMQ 诱导的 ICD 细胞裂解物介导的抗肿瘤免疫,这些癌细胞在体外对 IMQ 耐药。我们得出结论,IMQ 是一种真正的 ICD 诱导剂,并提供了一个将 IMQ 诱导的癌细胞死亡与抗肿瘤免疫反应联系起来的概念。

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